Term:Brugada syndrome 9
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Accession:DOID:0110226 term browser browse the term
Definition:A Brugada syndrome that has material basis in heterozygous mutation in the KCND3 gene on chromosome 1p13. (DO)
Synonyms:exact_synonym: BRGDA9
 primary_id: OMIM:616399
 alt_id: RDO:9001381
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Brugada syndrome 9 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kcnd3 potassium voltage-gated channel subfamily D member 3 JBrowse link 2 207,923,775 208,140,727 RGD:7240710
G Lama4 laminin subunit alpha 4 JBrowse link 20 44,060,715 44,201,966 RGD:8554872

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  disease 14875
    syndrome 4220
      Brugada syndrome 50
        Brugada syndrome 9 2
Path 2
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  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        genetic disease 5997
          monogenic disease 2855
            autosomal genetic disease 2137
              autosomal dominant disease 1098
                Brugada syndrome 9 2
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